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Kuhl, A.3
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LeBrazidec, J.-Y.1
Kocienski, P.J.2
Connolly, J.D.3
Muir, K.W.4
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28
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76449095986
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For few recent contributions see
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For few recent contributions see
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43
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25144433337
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These diastereomers were mentioned to be partially separable. See Complete separation was not achieved (chromatography/recrystallization) to proceed further with single diastereomer
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These diastereomers were mentioned to be partially separable. See. Harrowven D.C., Pascoe D.D., Demurtas D., and Bourne H.O. Angew. Chem., Int. Ed. 117 (2005) 1247-1248 Complete separation was not achieved (chromatography/recrystallization) to proceed further with single diastereomer
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(2005)
Angew. Chem., Int. Ed.
, vol.117
, pp. 1247-1248
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Harrowven, D.C.1
Pascoe, D.D.2
Demurtas, D.3
Bourne, H.O.4
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45
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0000914258
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No attempts were made to study the product for prediction of the type of reaction involved. Based on the following reference we call this reaction as an intramolecular Diels-Alder cyclization reaction as is catalyzed by Lewis acid. See
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No attempts were made to study the product for prediction of the type of reaction involved. Based on the following reference we call this reaction as an intramolecular Diels-Alder cyclization reaction as is catalyzed by Lewis acid. See Little, R.D.; Masjedizadeh, M. R.; Wallquist, O.; Mc. Loughlin, J.I. Org. React. 1995, 47, 315-551.
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(1995)
Org. React
, vol.47
, pp. 315-551
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Little, R.D.1
Masjedizadeh, M.R.2
Wallquist, O.3
Mc4
Loughlin, J.I.5
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47
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76449118378
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note
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-1, F(000)=560, λ=0.71073 Å. Data collection yielded 13,378 reflections resulting in 2493 unique, averaged reflection, 2031 with I>2σ(I). Full-matrix least-squares refinement led to a final R=0.0480, wR=0.1265, and GOF=1.020. Intensity data were measured on Bruker Smart Apex with CCD area detector. CCDC 741295 contains Supplementary crystallographic data for the structure.
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48
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76449105702
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note
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Attempts in ethanol, methanol, and combination of hexane/diethyl ether solutions did not yield the required crystal.
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